ARHGAP20
Rho GTPase activating protein 20
Summary
The protein encoded by this gene is an activator of RHO-type GTPases, transducing a signal from RAP1 to RHO and impacting neurite outgrowth. [provided by RefSeq, Sep 2016]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2134769388 | 11:110,450,117 | T/C | — | uncertain significance |
| rs190416825 | 11:110,450,144 | G/A | — | uncertain significance |
| rs201024136 | 11:110,450,266 | A/T | — | uncertain significance |
| rs142882906 | 11:110,450,297 | G/T | — | uncertain significance |
| rs780300469 | 11:110,450,404 | T/C | — | uncertain significance |
| rs139127000 | 11:110,450,449 | G/T | — | uncertain significance |
| rs748178488 | 11:110,450,489 | C/T | — | uncertain significance |
| rs1947391798 | 11:110,450,518 | T/C | — | uncertain significance |
| rs768150332 | 11:110,450,533 | T/C | — | uncertain significance |
| rs1343543554 | 11:110,450,635 | C/T | — | likely benign |
| rs199551649 | 11:110,450,672 | C/T | — | uncertain significance |
| rs1780612053 | 11:110,450,678 | C/A | — | uncertain significance |
| rs2539718642 | 11:110,450,776 | A/C | — | uncertain significance |
| rs758915435 | 11:110,450,885 | G/A | — | uncertain significance |
| rs1565417201 | 11:110,451,016 | A/T | — | uncertain significance |
| rs145371077 | 11:110,451,041 | G/A | — | uncertain significance |
| rs148615316 | 11:110,451,106 | C/A | — | uncertain significance |
| rs2539720168 | 11:110,451,120 | T/C | — | uncertain significance |
| rs763095486 | 11:110,451,121 | A/G | — | uncertain significance |
| rs373621632 | 11:110,451,142 | C/T | — | uncertain significance |
| rs202088486 | 11:110,451,283 | G/C | — | uncertain significance |
| rs755925518 | 11:110,451,302 | C/T | — | likely benign |
| rs142038774 | 11:110,451,391 | C/T | — | uncertain significance |
| rs368565272 | 11:110,451,545 | C/T | — | uncertain significance |
| rs773384110 | 11:110,451,584 | T/G | — | uncertain significance |
| rs369212996 | 11:110,451,659 | G/A | — | uncertain significance |
| rs751819482 | 11:110,451,665 | G/T | — | uncertain significance |
| rs150557417 | 11:110,451,694 | G/A | — | uncertain significance |
| rs563325668 | 11:110,451,884 | C/T | — | uncertain significance |
| rs1179890774 | 11:110,453,093 | G/A | — | uncertain significance |
| rs374173338 | 11:110,454,286 | C/T | — | uncertain significance |
| rs2539729872 | 11:110,454,358 | A/G | — | uncertain significance |
| rs148592330 | 11:110,461,382 | G/C | — | uncertain significance |
| rs377077772 | 11:110,461,422 | C/T | — | uncertain significance |
| rs1358193304 | 11:110,462,814 | T/C | — | uncertain significance |
| rs773586201 | 11:110,462,822 | C/T | — | uncertain significance |
| rs138162229 | 11:110,463,094 | G/T | intron variant | — |
| rs111236514 | 11:110,477,296 | T/G | — | uncertain significance |
| rs769722872 | 11:110,477,300 | C/G | — | uncertain significance |
| rs1565434839 | 11:110,477,303 | C/T | — | uncertain significance |
| rs762653052 | 11:110,477,315 | T/A | — | uncertain significance |
| rs2539778006 | 11:110,477,336 | A/G | — | uncertain significance |
| rs371577495 | 11:110,477,347 | C/A | — | uncertain significance |
| rs749855783 | 11:110,485,311 | C/T | — | uncertain significance |
| rs376005160 | 11:110,485,365 | T/G | — | uncertain significance |
| rs193920992 | 11:110,494,925 | A/G | — | uncertain significance |
| rs326946 | 11:110,499,253 | A/C | intron variant | — |
| rs147369246 | 11:110,501,424 | G/A | — | uncertain significance |
| rs138034862 | 11:110,501,432 | C/T | — | uncertain significance |
| rs34577374 | 11:110,501,433 | G/C | — | uncertain significance |
| rs1948842565 | 11:110,501,441 | A/G | — | uncertain significance |
| rs45605035 | 11:110,501,502 | C/T | — | uncertain significance |
| rs35391917 | 11:110,557,862 | A/G | intron variant | — |
| rs180920417 | 11:110,561,271 | T/C | — | uncertain significance |
| rs1950222904 | 11:110,561,306 | A/G | — | uncertain significance |
| rs1040881280 | 11:110,582,854 | T/C | — | uncertain significance |
| rs530582931 | 11:110,582,869 | C/A | — | uncertain significance |
| rs1950679489 | 11:110,582,896 | G/A | — | uncertain significance |
| rs1950680596 | 11:110,582,923 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.